Zhang Bing-Wei, Xu Jing, Chang Yi
Department of Neurology and Psychiatry, First Affiliated Hospital of Dalian Medical UniversityDalian, Liaoning, China; Translational Medicine Research Center of Nerve System DiseaseDalian, Liaoning, China.
Department of Neurology and Psychiatry, First Affiliated Hospital of Dalian Medical University Dalian, Liaoning, China.
Front Hum Neurosci. 2016 Mar 30;10:116. doi: 10.3389/fnhum.2016.00116. eCollection 2016.
Elderly depressed patients manifest pronounced executive dysfunction compared with younger subjects with depressive disorder. Aging-related brain changes may result in executive dysfunction in geriatric depression. We investigated the neural correlates of inhibitory control processing in depressed subjects at different ages using event-related potentials (ERPs). A equiprobable visual Go/Nogo task was used in 19 young (27.4 ± 5.0 years) and 18 elderly (70.8 ± 6.9 years) depressed subjects and their age-matched healthy controls (20 young subjects, 26.2 ± 3.7 years, and 18 elderly subjects, 68.1 ± 4.8 years). The responses were based on two types of equilateral triangular figures of upright (Go) and inverted triangle (Nogo). The elderly subjects exhibited later N2 and P3 latencies, and larger Go-N2 and P3 amplitudes, compared with the younger subjects. Further, the elderly controls displayed smaller P3 in the central and parietal regions, and yielded larger Nogo-P3 amplitude in the frontal region compared with younger controls. While the young depressed patients yielded smaller P3 amplitude than the controls across frontal, central and parietal regions, elderly depressed patients yielded smaller P3 than the elderly controls only in the frontal region. Our results suggest that the inhibitory control subprocesses are differentially affected by depression and aging. The stimulus response speed and the effort intensity of inhibition control are specifically impaired in the elderly depressed patients. And the diminished amplitudes of frontal P3 in the elderly depression imply a frontal dysfunction mechanism.
与患有抑郁症的年轻受试者相比,老年抑郁症患者表现出明显的执行功能障碍。与衰老相关的大脑变化可能导致老年抑郁症患者出现执行功能障碍。我们使用事件相关电位(ERP)研究了不同年龄段抑郁症患者抑制控制加工的神经相关性。对19名年轻(27.4±5.0岁)和18名老年(70.8±6.9岁)抑郁症患者及其年龄匹配的健康对照者(20名年轻受试者,26.2±3.7岁,18名老年受试者,68.1±4.8岁)进行了等概率视觉Go/Nogo任务测试。反应基于两种类型的等边三角形图形,直立三角形(Go)和倒三角形(Nogo)。与年轻受试者相比,老年受试者的N2和P3潜伏期更晚,Go-N2和P3波幅更大。此外,与年轻对照者相比,老年对照者在中央和顶叶区域的P3较小,而在额叶区域的Nogo-P3波幅更大。虽然年轻抑郁症患者在额叶、中央和顶叶区域的P3波幅均小于对照者,但老年抑郁症患者仅在额叶区域的P3小于老年对照者。我们的结果表明,抑制控制子过程受抑郁症和衰老的影响不同。老年抑郁症患者的刺激反应速度和抑制控制的努力强度受到特异性损害。老年抑郁症患者额叶P3波幅减小意味着存在额叶功能障碍机制。